Canonical Allele Identifier: CA1675538418

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190126_157190164delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG , CM000668.2:g.157190126_157190164delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	GRCh38
NC_000006.11:g.157511260_157511298delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG , CM000668.1:g.157511260_157511298delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	GRCh37
NC_000006.10:g.157552952_157552990delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	NCBI36
NG_032093.1:g.417197_417235delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG
NG_032093.2:g.417197_417235delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG
NG_066624.1:g.419101_419139delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3988_4026delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	ENSP00000055163.8:p.Tyr1330=
ENST00000414678.8:c.4057_4095delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	ENSP00000412835.3:p.Tyr1353=
ENST00000637015.2:c.4276_4314delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	ENSP00000489729.2:p.Tyr1426=
ENST00000346085.10:c.4027_4065delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	ENSP00000344546.5:p.Tyr1343=
ENST00000350026.10:c.3739_3777delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	ENSP00000055163.7:p.Tyr1247=
ENST00000414678.7:c.2305_2343delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	ENSP00000412835.2:p.Tyr769=
ENST00000635849.1:c.1468_1506delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	ENSP00000490948.1:p.Tyr490=
ENST00000635957.1:c.1099_1137delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	ENSP00000490385.1:p.Tyr367=
ENST00000636930.2:c.4147_4185delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG MANE Select	ENSP00000490491.2:p.Tyr1383=
ENST00000636940.1:n.2144_2182delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG
ENST00000637015.1:c.1515_1553delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG
ENST00000637568.1:c.1429_1467delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG
ENST00000637741.1:n.813_851delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG
ENST00000637810.1:c.1489_1527delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	ENSP00000489636.1:p.Tyr497=
ENST00000637904.1:c.1648_1686delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	ENSP00000490550.1:p.Tyr550=
ENST00000647938.1:c.3778_3816delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	ENSP00000498155.1:p.Tyr1260=
ENST00000346085.9:c.3778_3816delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	ENSP00000344546.4:p.Tyr1260=
ENST00000350026.9:c.3739_3777delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	ENSP00000055163.7:p.Tyr1247=
ENST00000414678.6:c.2305_2343delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	ENSP00000412835.2:p.Tyr769=
NM_017519.2:c.3739_3777delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	NP_059989.2:p.Tyr1247=
NM_020732.3:c.3778_3816delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	NP_065783.3:p.Tyr1260=
XM_005267069.3:c.3898_3936delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	XP_005267126.2:p.Tyr1300=
XM_011535984.1:c.2977_3015delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	XP_011534286.1:p.Tyr993=
XM_011535985.1:c.2797_2835delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	XP_011534287.1:p.Tyr933=
XM_011535986.1:c.2557_2595delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	XP_011534288.1:p.Tyr853=
XM_011535987.1:c.2176_2214delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	XP_011534289.1:p.Tyr726=
XM_011535988.1:c.1039_1077delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	XP_011534290.1:p.Tyr347=
NM_001346813.1:c.3898_3936delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	NP_001333742.1:p.Tyr1300=
NM_001363725.1:c.1648_1686delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	NP_001350654.1:p.Tyr550=
XM_011535984.2:c.4108_4146delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	XP_011534286.2:p.Tyr1370=
XM_011535988.3:c.1039_1077delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	XP_011534290.1:p.Tyr347=
XM_017011103.2:c.4009_4047delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	XP_016866592.1:p.Tyr1337=
XM_017011104.1:c.3979_4017delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	XP_016866593.1:p.Tyr1327=
XM_017011105.2:c.3949_3987delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	XP_016866594.1:p.Tyr1317=
XM_017011106.2:c.3820_3858delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	XP_016866595.1:p.Tyr1274=
XM_017011107.2:c.3799_3837delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	XP_016866596.1:p.Tyr1267=
XR_002956289.1:n.4191_4229delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG
NM_001363725.2:c.1648_1686delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	NP_001350654.1:p.Tyr550=
NM_001371656.1:c.4027_4065delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	NP_001358585.1:p.Tyr1343=
NM_001374820.1:c.4027_4065delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	NP_001361749.1:p.Tyr1343=
NM_001374828.1:c.4147_4185delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG MANE Select	NP_001361757.1:p.Tyr1383=
NM_017519.3:c.3988_4026delinsTACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG	NP_059989.3:p.Tyr1330=